Heparin/heparan sulphate interactions with complement-a possible target for reduction of renal function loss?

被引:37
作者
Zaferani, Azadeh [1 ]
Talsma, Ditmer [1 ]
Richter, Mareike K. S. [1 ]
Daha, Mohamed R. [1 ]
Navis, Gerjan J. [1 ]
Seelen, Marc A. [1 ]
van den Born, Jacob [1 ]
机构
[1] Univ Groningen, Univ Med Ctr Groningen, Dept Internal Med, Div Nephrol, Groningen, Netherlands
关键词
complement system; proteoglycans; renal failure; HEPARAN-SULFATE; FACTOR-H; PROTEIN INTERACTIONS; ALTERNATIVE PATHWAY; ALLOGRAFT-REJECTION; REPERFUSION INJURY; BINDING-SITE; C1; INHIBITOR; ACTIVATION; GLYCOSAMINOGLYCANS;
D O I
10.1093/ndt/gft243
中图分类号
R3 [基础医学]; R4 [临床医学];
学科分类号
1001 ; 1002 ; 100602 ;
摘要
Current management of end-stage renal failure is based on renal replacement therapy by dialysis or transplantation. Increased occurrence of renal failure in both native and transplanted kidneys indicates a need for novel therapies to stop or limit the progression of the disease. Acute kidney injury and proteinuria are major risk factors in the development of renal failure. In this regard, innate immunity plays an important role in the pathogenesis of renal diseases in both native and transplanted kidneys. The complement system is a major humoral part of innate defense. Next to the well-known complement activators, quite a number of the complement factors react with proteoglycans (PGs) both on cellular membranes and in the extracellular compartment. Therefore, these interactions might serve as targets for intervention. In this review, the current knowledge of interactions between PGs and complement is reviewed, and additionally the options for interference in the progression of renal disease are discussed.
引用
收藏
页码:515 / 522
页数:8
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